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枯草芽孢杆菌DNA聚合酶III:polC基因的完整序列、过表达及特性分析

Bacillus subtilis DNA polymerase III: complete sequence, overexpression, and characterization of the polC gene.

作者信息

Hammond R A, Barnes M H, Mack S L, Mitchener J A, Brown N C

机构信息

Department of Pharmacology, University of Massachusetts Medical School, Worcester 01655.

出版信息

Gene. 1991 Feb 1;98(1):29-36. doi: 10.1016/0378-1119(91)90100-p.

Abstract

Genomic DNA encompassing polC, the structural gene specifying Bacillus subtilis DNA polymerase III (PolIII), was sequenced and found to contain a 4311-bp open reading frame (ORF) encoding a 162.4-kDa polypeptide of 1437 amino acids (aa). The ORF was engineered into an Escherichia coli expression plasmid under the control of the coliphage lambda repressor. Derepression of E. coli transformants carrying the recombinant vector resulted in the high-level synthesis of a recombinant DNA polymerase indistinguishable from native PolIII. N-terminal aa sequence analysis of the recombinant polymerase unequivocally identified the 4311-bp ORF as that of polC. Comparative aa sequence analysis indicated significant homology of the B. subtilis enzyme with the catalytic alpha subunit of the E. coli PolIII and, with the exception of an exonuclease domain, little homology with other DNA polymerases. The respective sequences of the mutant polC alleles, dnaF and ts-6, were identified, and the expression of specifically truncated forms of polC was exploited to assess the dependence of polymerase activity on the structure of the enzyme's C terminus.

摘要

对包含polC的基因组DNA进行了测序,polC是编码枯草芽孢杆菌DNA聚合酶III(PolIII)的结构基因,发现其含有一个4311碱基对的开放阅读框(ORF),编码一个由1437个氨基酸(aa)组成的162.4 kDa多肽。该ORF被构建到一个在噬菌体λ阻遏物控制下的大肠杆菌表达质粒中。携带重组载体的大肠杆菌转化体的去阻遏导致了一种与天然PolIII无法区分的重组DNA聚合酶的高水平合成。对重组聚合酶的N端氨基酸序列分析明确鉴定出4311碱基对的ORF为polC的ORF。比较氨基酸序列分析表明,枯草芽孢杆菌的这种酶与大肠杆菌PolIII的催化α亚基有显著同源性,并且除了一个核酸外切酶结构域外,与其他DNA聚合酶的同源性很小。确定了突变型polC等位基因dnaF和ts - 6的各自序列,并利用polC特异性截短形式的表达来评估聚合酶活性对酶C末端结构的依赖性。

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